rs25487, XRCC1

N. diseases: 205
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Childhood Acute Lymphoblastic Leukemia
261 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 1.000 10 2007 2015
Congenital chromosomal disease
CUI: C0008626
Disease: Congenital chromosomal disease
47 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.060 1.000 6 2004 2012
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.050 1.000 5 2012 2017
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.040 1.000 4 2006 2016
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.040 1.000 4 2006 2016
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2008 2016
Carcinoma of larynx
CUI: C0595989
Disease: Carcinoma of larynx
65 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2014 2016
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2013 2018
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2012 2016
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2013 2015
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2007 2017
Glaucoma, Primary Open Angle
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
222 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2011 2015
leukemia
CUI: C0023418
Disease: leukemia
144 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2013 2015
Malignant neoplasm of larynx
CUI: C0007107
Disease: Malignant neoplasm of larynx
50 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2014 2016
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2013 2018
Rectal Carcinoma
CUI: C0007113
Disease: Rectal Carcinoma
112 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2010 2011
Skin carcinoma
CUI: C0699893
Disease: Skin carcinoma
24 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2002 2017
Sporadic Breast Carcinoma
CUI: C1336076
Disease: Sporadic Breast Carcinoma
46 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2007 2015
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
82 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2005 2015
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 1.000 2 2005 2010
Adenocarcinoma Of Esophagus
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
81 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 1.000 2 2005 2007
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
98 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 1.000 2 2013 2016
Age-related cataract
CUI: C0036646
Disease: Age-related cataract
15 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 1.000 2 2015 2015
Barrett Esophagus
CUI: C0004763
Disease: Barrett Esophagus
60 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 1.000 2 2005 2008
Carcinoma, Transitional Cell
CUI: C0007138
Disease: Carcinoma, Transitional Cell
12 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 1.000 2 2014 2015